Medical Director-Oncology Clinical Development - GI

Job description

Description

For candidates seeking to be located at our Stevenage site, this role will temporarily be based at Stevenage. However, the Company plans to relocate its offices to Cambridge, UK. The location of this role will therefore subsequently change to Cambridge, UK in accordance with timelines to be set by the Company. The relocation is currently proposed to take effect by early 2029.

Overview

Cancer is unrelenting, but so are we. At GSK, we are committed to transforming outcomes for people with cancer through innovative science, bold ambition, and strong partnerships across the healthcare ecosystem. We focus our science where it can matter most - advancing care in cancers with high unmet need, grounded in a deep understanding of disease biology and deliberate scientific choices that connect discovery to meaningful impact in the real world.

Medical Director, Oncology Clinical Development - GI

is the physician within the clinical programme team, bringing medical expertise, clinical judgement, and a patient-centred perspective to the design, conduct, and interpretation of clinical studies. This role is accountable for medical monitoring and safety oversight, ensuring that patient safety and clinical integrity are maintained throughout study execution.

Operating within the clinical strategy defined by the Clinical Development Lead (CDL), the Medical Director partners closely with the Senior Scientist and cross-functional teams to ensure that the physician perspective is fully integrated into study delivery. The role serves as a core member of the Clinical Matrix Team (CMT), contributing to study-level decisions, investigator engagement, and regulatory interactions.

For more complex or multi-study programmes, the Medical Director may provide medical guidance to other physicians within the programme and contribute to broader clinical discussions that inform programme-level decisions led by the CDL.

In This Role You Will:

Serve as the physician within the clinical programme team, providing medical expertise across study design, conduct, safety oversight, and data interpretation

Lead medical monitoring activities for clinical studies, ensuring patient safety, clinical integrity, and compliance with the protocol and regulatory requirements

Interpret clinical and safety data from a physician perspective, generating insights that inform study-level and programme-level decisions led by the CDL

Partner with the Senior Scientist and cross-functional teams to ensure medical considerations are integrated into study execution and delivery

Contribute medical expertise to protocol development, ensuring clinical relevance, patient safety, and feasibility within the framework defined by the CDL

Serve as a core member of the Clinical Matrix Team (CMT), providing the medical voice in study-level discussions and cross-functional decision-making

Engage with investigators and Key External Experts (KEEs) to support study conduct, scientific exchange, and external representation of the programme

Contribute to regulatory documents, Health Authority interactions, and scientific communications from a physician perspective

Detailed Responsibilities:

Medical Monitoring and Safety Oversight

Lead medical monitoring activities for assigned clinical studies, including real-time clinical decision-making on patient eligibility, protocol-related medical queries, and safety oversight

Conduct and oversee medical review of clinical trial data, both directly and through oversight of delegated medical review activities

Interpret and contextualise safety data in collaboration with pharmacovigilance, ensuring appropriate signal detection, escalation, and benefit-risk assessment at the study level

Participate in safety review forums, including Safety Review Team (SRT) discussions, Independent Data Monitoring Committee (IDMC) data reviews, and internal governance as required

Ensure medical monitoring activities are conducted in compliance with GCP, ICH guidelines, and applicable regulatory frameworks

Study Design and Execution

Provide medical input into protocol development, ensuring clinical relevance, patient safety, and operational feasibility within the clinical strategy defined by the CDL

Apply clinical judgement to support protocol implementation, addressing medical questions that arise during study conduct and ensuring consistency with the study's scientific objectives

Partner with the Senior Scientist to ensure that medical considerations are fully integrated into study execution, data generation, and operational delivery

Contribute to the development and review of key study documents, including the Informed Consent Form (ICF), protocol deviation management plan (PDMP), and study reference manual (SRM)

Provide medical input into clinical data generation activities, ensuring alignment with study objectives, patient safety considerations, and the Clinical Development Plan (CDP)

Data Interpretation and Scientific Contribution

Interpret clinical data from a physician perspective, translating findings into insights on safety, efficacy, and patient impact that inform decision-making by the CDL

Contribute to study-level and programme-level data interpretation, supporting the CDL's assessment of benefit-risk and clinical positioning

Contribute to the development of scientific communications, including study reports, clinical study summaries, publications, and congress materials

Collaborate with investigators on the evaluation and development of abstracts, posters, and manuscripts derived from clinical programme data

Maintain current knowledge of the asset's biological mechanism, disease landscape, evolving treatment paradigms, and competitive environment to inform clinical interpretation

Regulatory and External Engagement

Contribute medical expertise to regulatory documents and Health Authority interactions, including responses to clinical and safety queries

Support preparation of materials for regulatory submissions, advisory boards, and external engagements, providing the physician perspective on clinical data and safety

Engage with Key External Experts (KEEs), investigators, and scientific collaborators to support study conduct, scientific exchange, and relationship development

Represent the medical perspective at cross-departmental interactions, including Integrated Evidence Team (IET) and Medical Affairs strategy discussions, as delegated by the CDL

Contribute to the clinical and technical diligence assessment of business development opportunities as requested

Cross-Functional Collaboration and Clinical Matrix Team

Serve as a core member of the Clinical Matrix Team (CMT), providing medical leadership within study execution

Contribute medical expertise to disease area strategy, integrated evidence planning, and Medical Affairs discussions as appropriate

Collaborate across functions - including Clinical Operations, Biostatistics, Regulatory, and Pharmacovigilance - to ensure alignment on study objectives, patient safety, and data quality

Contribute to Oncology Clinical Development-wide initiatives and workstreams

Working Model

This role is hybrid and based in Switzerland. You will be expected to be on-site regularly and collaborate with colleagues across locations.

Basic Qualifications

MD (or equivalent medical degree) with board certification or eligibility in oncology, haematology, or a related specialty

Clinical experience in oncology and/or relevant therapeutic areas, with direct exposure to clinical research or drug development

Demonstrated experience in clinical trial conduct, including medical monitoring, safety review, and clinical data interpretation

Strong working knowledge of clinical development processes, including GCP, ICH guidelines, and global regulatory frameworks

Ability to apply clinical judgement to support study design, patient safety, and real-time medical decision-making within a structured clinical development framework

Experience operating effectively within cross-functional matrix teams in a pharmaceutical, biotechnology, or academic clinical trial environment

Strong scientific communication skills, with the ability to translate clinical data into clear insights for internal and external audiences

Preferred Qualifications

Experience in pharmaceutical or biotechnology clinical development across Phase I-III GI oncology studies

Prior experience contributing to regulatory interactions (e.g., IND submissions, scientific advice, NDA/MAA filings)

Demonstrated experience engaging with Key External Experts (KEEs), investigators, and scientific collaborators in oncology

Track record of contributing to clinical publications, congress presentations, or scientific communications

Deep understanding of oncology disease biology, evolving treatment paradigms, and the competitive landscape across solid tumours and/or haematological malignancies

Experience in medical monitoring across multiple studies or programmes within a clinical development organisation

Familiarity with emerging data and analytics approaches (e.g., real-world evidence, AI-enabled insights) to support clinical interpretation and decision-making

What we value in you

We act with transparency, respect and integrity. We welcome different perspectives and champion inclusion. Bring curiosity, humility and a clear focus on patients. If you are motivated to drive clinical progress and to grow with a team that values collaboration and impact, we encourage you to apply.

Skills

Analytical Thinking, Clinical Data Interpretation, Clinical Development, Clinical Pharmacology, Clinical Trial Designs, Clinical Trials Monitoring,

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Who can apply

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